Evidence map›Paper›PMID 36975511›Full record

ReviewCurrent issues in molecular biology2023

Advances in Ion Channel, Non-Desmosomal Variants and Autophagic Mechanisms Implicated in Arrhythmogenic Cardiomyopathy.

Kexin Li, Yufeng Jiang, Yiyao Zeng, Yafeng Zhou

Open access · goldFull text readReview
In one paragraph

Review in Current issues in molecular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.1field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Kexin LiDepartment of Cardiology, Dushu Lake Hospital Affiliated to Soochow University, Suzhou 215000, China.
Yufeng JiangDepartment of Cardiology, Dushu Lake Hospital Affiliated to Soochow University, Suzhou 215000, China.ORCID 0000-0003-4553-4834
Yiyao ZengDepartment of Cardiology, Dushu Lake Hospital Affiliated to Soochow University, Suzhou 215000, China.
Yafeng ZhouDepartment of Cardiology, Dushu Lake Hospital Affiliated to Soochow University, Suzhou 215000, China.
Soochow University · CN

Funding

Clinical Medicine Expert Team (Class A) of Jinji Lake Health Talents Program of Suzhou Indus-trial Park SZYQTD202102Demonstration of Scientific and Technological Innovation Project SKY2021002National Natural Science Foundation of China 81873486Research on Collaborative Innovation of medical engineering combination SZM2021014Suzhou Dedicated Project on Diagnosis and Treatment Technology of Major Diseases LCZX202132Suzhou Key Discipline for Medicine SZXK202129the Science and Technology Development Program of Jiangsu Province-Clinical Frontier Tech-nology BE2022754
6 · The paper itself

Abstract

Arrhythmogenic cardiomyopathy (ACM) is a heterogeneous disorder characterized by the replacement of cardiac myocytes with fibro-fatty tissues, leading to abnormal excitation-contraction (EC) coupling and a range of malignant events, such as ventricular tachycardia (VT), sudden cardiac death/arrest (SCD/A) and heart failure (HF). The concept of ACM has recently been ex-tended to include right ventricular cardiomyopathy (ARVC), left ventricular cardiomyopathy (ALVC) and biventricular cardiomyopathy. ARVC is generally seen as the most common type of ACM. The pathogenesis of ACM involves mutation variants in desmosomal or non-desmosomal gene loci, as well as various external factors, such as intense exercise, stress and infections. Ion channel alterations, autophagy and non-desmosomal variants are also important components in the development of ACM. As clinical practice enters the era of precision therapy, it is important to review recent studies on these topics to better diagnose and treat the molecular phase of ACM.

Indexed as

arrhythmogenic cardiomyopathyautophagyion channelnon-desmosomal variant

Identifiers

PMID36975511
PMCPMC10047275
OpenAlexW4323569626

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read3
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.